Canonical Allele Identifier: CA418438636

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724622A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258939A>T , CM000663.2:g.67258939A>T	GRCh38
NC_000001.10:g.67724622A>T , CM000663.1:g.67724622A>T	GRCh37
NC_000001.9:g.67497210A>T	NCBI36
NG_011498.1:g.97454A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1540A>T	ENSP00000513138.1:n.1540A>T
ENST00000697150.1:c.1598A>T	ENSP00000513139.1:n.1598A>T
ENST00000697151.1:c.1531A>T	ENSP00000513140.1:n.1531A>T
ENST00000697164.1:c.1611A>T	ENSP00000513153.1:p.Val537=
ENST00000697165.1:c.1398A>T	ENSP00000513154.1:p.Val466=
ENST00000347310.10:c.1701A>T MANE Select	ENSP00000321345.5:p.Val567=
ENST00000637002.1:c.1092A>T	ENSP00000490340.1:p.Val364=
ENST00000347310.9:c.1701A>T	ENSP00000321345.5:p.Val567=
ENST00000395227.2:c.495A>T	ENSP00000378652.2:p.Val165=
ENST00000425614.3:c.936A>T	ENSP00000387640.2:p.Val312=
ENST00000473881.2:c.*527A>T	ENSP00000486667.1:n.*527A>T
NM_144701.2:c.1701A>T	NP_653302.2:p.Val567=
XM_005270516.2:c.939A>T	XP_005270573.1:p.Val313=
XM_011540789.1:c.1791A>T	XP_011539091.1:p.Val597=
XM_011540790.1:c.1701A>T	XP_011539092.1:p.Val567=
XM_011540791.1:c.1701A>T	XP_011539093.1:p.Val567=
XM_011540790.3:c.1701A>T	XP_011539092.1:p.Val567=
XM_011540791.3:c.1701A>T	XP_011539093.1:p.Val567=
XR_001736993.1:n.1781A>T
NM_144701.3:c.1701A>T MANE Select	NP_653302.2:p.Val567=